Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Ehab Abdelkader"'
Autor:
Abdulaziz A. Alshamrani, Osama Raddadi, Patrik Schatz, Steffen Lenzner, Christine Neuhaus, Eman Azzam, Ehab Abdelkader
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 19, Iss , Pp 100780- (2020)
Purpose: To report a severe phenotype of retinitis pigmentosa associated with novel mutations in CNGB1. Observations: Six siblings, age range 50–75 years old, were examined using optical coherence tomography and fundus autofluorescene, electroretin
Externí odkaz:
https://doaj.org/article/a1e3445a697c41f3bb31b74cc1cdac30
Publikováno v:
Journal of Medical Case Reports, Vol 11, Iss 1, Pp 1-5 (2017)
Abstract Background Proliferative diabetic retinopathy is a major cause of visual impairment in working-age adults worldwide. Panretinal photocoagulation is a cornerstone in its management; however, it may include a range of side effects and complica
Externí odkaz:
https://doaj.org/article/7b61510ddf814d2bb687ec8a9302b45c
Autor:
Vaibhav Vats, Aarij Elahi, Sinda Hidri, Rem Ehab Abdelkader, Farhan Munaf, Jennifer Mercika Prince, Muhammad Ahsan Asif, Huzaifa Ahmad Cheema, Adeel Ahmad, Wajeeh Ur Rehman, Abdulqadir J. Nashwan, Raheel Ahmed, Vladimir Lakhter, Hafeez Ul Hassan Virk, Royce P. Vincent
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
BackgroundOptical coherence tomography (OCT) and intravascular ultrasound (IVUS) are superior to coronary angiography for guiding percutaneous coronary intervention (PCI). However, whether one technique is superior to the other is inconclusive.Method
Externí odkaz:
https://doaj.org/article/515a4bb22de84fbe9a84a431acb4417b
Publikováno v:
Innovative Infrastructure Solutions. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8870c9577dd191251339f2447fde972e
https://doi.org/10.1007/s41062-022-00872-2
https://doi.org/10.1007/s41062-022-00872-2
Publikováno v:
RETINAL Cases & Brief Reports. 14:203-210
PURPOSE: To describe a specific cone-rod dystrophy phenotype in a family with the homozygous c.1429G>A; p.Gly477Arg mutation in CRB1. The detailed phenotype of subjects with this specific mutation has not been described previously. METHODS: Clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d462bd638c98b2a49acd3a72a98e8bb
https://doi.org/10.1097/icb.0000000000000654
https://doi.org/10.1097/icb.0000000000000654
Publikováno v:
Saudi Journal of Ophthalmology, Vol 33, Iss 1, Pp 61-65 (2019)
Purpose: To report anatomical and visual outcomes of Nd:YAG laser posterior hyaloidotomy (NYPH) in Saudi patients affected by Premacular subhyaloid haemorrhage (PMSHH). Methods: 8 eyes from 8 patients (7 males and one female) were treated with NYPH w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77d54c5828a38998392dea2bde9f45f9
https://doi.org/10.1016/j.sjopt.2018.11.007
https://doi.org/10.1016/j.sjopt.2018.11.007
Autor:
Osama Raddadi, Eman Azzam, Abdulaziz A Alshamrani, Christine Neuhaus, Patrik Schatz, Steffen Lenzner, Ehab Abdelkader
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 19, Iss, Pp 100780-(2020)
American Journal of Ophthalmology Case Reports
American Journal of Ophthalmology Case Reports
Purpose: To report a severe phenotype of retinitis pigmentosa associated with novel mutations in CNGB1. Observations: Six siblings, age range 50–75 years old, were examined using optical coherence tomography and fundus autofluorescene, electroretin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d57a0336b67e2739b7f5941b19c6e01c
http://www.sciencedirect.com/science/article/pii/S2451993618305048
http://www.sciencedirect.com/science/article/pii/S2451993618305048
Construction of the Ethiopian Grand Renaissance dam (GRD) has many impacts and implication on the water share and future use in Egypt. Especially the period of the reservoir filling will have a great effect on the Nile River and its water in Egypt. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::827a5a638ed3d491e35ceb5cee09b59a
https://doi.org/10.21203/rs.3.rs-30307/v2
https://doi.org/10.21203/rs.3.rs-30307/v2
Publikováno v:
Saudi Journal of Ophthalmology, Vol 32, Iss 2, Pp 119-125 (2018)
Purpose: Usher syndrome is the most common cause of deafness associated with visual loss of a genetic origin. The purpose of this paper is to report very severe phenotypic features of type 1B Usher syndrome in a Saudi family affected by positive homo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24143592b207064842911d4bc4b8a0f4
http://www.sciencedirect.com/science/article/pii/S1319453417301327
http://www.sciencedirect.com/science/article/pii/S1319453417301327
Autor:
Al Anoud S. Aldrees, Ehab Abdelkader, Zuhair Rahbeeni, Patrik Schatz, Huda Al-Rwebah, Hussain Al-Habboubi
Publikováno v:
Ophthalmic Genetics. 40:77-79
Dear Editor,Alstrom syndrome (ALMS; MIM# 203800) is characterized by early onset cone-rod dystrophy (CRD), sensorineural hearing loss, obesity, cardiomyopathy, pulmonary disease, hepatic disease, r...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76a5ba7dfb5cc2329e151bf7c3f763ce
https://doi.org/10.1080/13816810.2018.1551495
https://doi.org/10.1080/13816810.2018.1551495